Senior Medical Writer: Regulatory Docs & Publications Lead

A healthcare communications company in Illinois seeks an experienced medical writer to lead complex writing projects for Clinical Research Scientists and external partners. The role involves creating regulatory documents, mentoring junior team members, and coordinating document reviews. Candidates should have 7-9 years of relevant medical writing experience, a strong background in CSRs and ICFs, and excellent communication skills. A commitment to continuous improvement and adaptability to new technologies is essential. #J-18808-Ljbffr